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Manganese causes neurotoxic iron accumulation via translational repression of amyloid precursor protein and H-Ferritin.

Authors :
Venkataramani V
Doeppner TR
Willkommen D
Cahill CM
Xin Y
Ye G
Liu Y
Southon A
Aron A
Au-Yeung HY
Huang X
Lahiri DK
Wang F
Bush AI
Wulf GG
Ströbel P
Michalke B
Rogers JT
Source :
Journal of neurochemistry [J Neurochem] 2018 Dec; Vol. 147 (6), pp. 831-848. Date of Electronic Publication: 2018 Nov 19.
Publication Year :
2018

Abstract

For more than 150 years, it is known that occupational overexposure of manganese (Mn) causes movement disorders resembling Parkinson's disease (PD) and PD-like syndromes. However, the mechanisms of Mn toxicity are still poorly understood. Here, we demonstrate that Mn dose- and time-dependently blocks the protein translation of amyloid precursor protein (APP) and heavy-chain Ferritin (H-Ferritin), both iron homeostatic proteins with neuroprotective features. APP and H-Ferritin are post-transcriptionally regulated by iron responsive proteins, which bind to homologous iron responsive elements (IREs) located in the 5'-untranslated regions (5'-UTRs) within their mRNA transcripts. Using reporter assays, we demonstrate that Mn exposure repressed the 5'-UTR-activity of APP and H-Ferritin, presumably via increased iron responsive proteins-iron responsive elements binding, ultimately blocking their protein translation. Using two specific Fe <superscript>2+</superscript> -specific probes (RhoNox-1 and IP-1) and ion chromatography inductively coupled plasma mass spectrometry (IC-ICP-MS), we show that loss of the protective axis of APP and H-Ferritin resulted in unchecked accumulation of redox-active ferrous iron (Fe <superscript>2+</superscript> ) fueling neurotoxic oxidative stress. Enforced APP expression partially attenuated Mn-induced generation of cellular and lipid reactive oxygen species and neurotoxicity. Lastly, we could validate the Mn-mediated suppression of APP and H-Ferritin in two rodent in vivo models (C57BL6/N mice and RjHan:SD rats) mimicking acute and chronic Mn exposure. Together, these results suggest that Mn-induced neurotoxicity is partly attributable to the translational inhibition of APP and H-Ferritin resulting in impaired iron metabolism and exacerbated neurotoxic oxidative stress. OPEN SCIENCE BADGES: This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.<br /> (© 2018 International Society for Neurochemistry.)

Details

Language :
English
ISSN :
1471-4159
Volume :
147
Issue :
6
Database :
MEDLINE
Journal :
Journal of neurochemistry
Publication Type :
Academic Journal
Accession number :
30152072
Full Text :
https://doi.org/10.1111/jnc.14580